Vance Wong - Publications

Affiliations: 
2001 University of Illinois, Urbana-Champaign, Urbana-Champaign, IL 

92 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Wong PT, Wong VC. Prevalence and Characteristics of Vaccination Triggered Seizures in Dravet Syndrome in Hong Kong: A Retrospective Study. Pediatric Neurology. PMID 26995069 DOI: 10.1016/j.pediatrneurol.2016.01.011  0.44
2015 Cheuk DK, Wong V, Wraige E, Baxter P, Cole A. Surgery for scoliosis in Duchenne muscular dystrophy. The Cochrane Database of Systematic Reviews. 10: CD005375. PMID 26423318 DOI: 10.1002/14651858.CD005375.pub4  0.44
2015 Wong VC, Fung CW, Lee SL, Wong PT. Review of evolution of clinical, training and educational services and research program for autism spectrum disorders in Hong Kong. Science China. Life Sciences. PMID 26335731 DOI: 10.1007/s11427-012-4294-y  0.44
2015 Kwong AK, Ho AC, Fung CW, Wong VC. Analysis of mutations in 7 genes associated with neuronal excitability and synaptic transmission in a cohort of children with non-syndromic infantile epileptic encephalopathy. Plos One. 10: e0126446. PMID 25951140 DOI: 10.1371/journal.pone.0126446  0.44
2015 Wong VC, Kwong AK. ATP1A3 mutation in a Chinese girl with alternating hemiplegia of childhood - Potential target of treatment? Brain & Development. PMID 25662428 DOI: 10.1016/j.braindev.2015.01.003  0.44
2015 Wong VC, Fung CW, Kwong AK. SCN2A mutation in a Chinese boy with infantile spasm - response to Modified Atkins Diet. Brain & Development. 37: 729-32. PMID 25459969 DOI: 10.1016/j.braindev.2014.10.008  0.44
2015 Wong VC, Kwong AK. CDKL5 variant in a boy with infantile epileptic encephalopathy: case report. Brain & Development. 37: 446-8. PMID 25085838 DOI: 10.1016/j.braindev.2014.07.003  0.44
2015 Xu J, Wong KSK, Wong V, Heisler M, Lee S, Cua M, Jian Y, Sarunic MV. Enhancing the visualization of human retina vascular networks by Graphics Processing Unit accelerated speckle variance OCT and graph cut retinal layer segmentation Progress in Biomedical Optics and Imaging - Proceedings of Spie. 9312. DOI: 10.1117/12.2081492  0.44
2015 Wong VCN. My 30-year roadmap for pediatric myasthenia gravis in Hong Kong: Searching for international collaboration Clinical and Experimental Neuroimmunology. 6: 13-20. DOI: 10.1111/cen3.12157  0.44
2015 Wong VCN, Fung CW, Lee SL, Wong PTY. Review of evolution of clinical, training and educational services and research program for autism spectrum disorders in Hong Kong Science China Life Sciences. DOI: 10.1007/s11427-012-4294-y  0.44
2014 Baum L, Haerian BS, Ng HK, Wong VC, Ng PW, Lui CH, Sin NC, Zhang C, Tomlinson B, Wong GW, Tan HJ, Raymond AA, Mohamed Z, Kwan P. Case-control association study of polymorphisms in the voltage-gated sodium channel genes SCN1A, SCN2A, SCN3A, SCN1B, and SCN2B and epilepsy. Human Genetics. 133: 651-9. PMID 24337656 DOI: 10.1007/s00439-013-1405-1  0.44
2014 Tso WW, Kwong AK, Fung CW, Wong VC. Folinic acid responsive epilepsy in Ohtahara syndrome caused by STXBP1 mutation. Pediatric Neurology. 50: 177-80. PMID 24315539 DOI: 10.1016/j.pediatrneurol.2013.10.006  0.44
2014 Bölte S, de Schipper E, Robison JE, Wong VC, Selb M, Singhal N, de Vries PJ, Zwaigenbaum L. Classification of functioning and impairment: the development of ICF core sets for autism spectrum disorder. Autism Research : Official Journal of the International Society For Autism Research. 7: 167-72. PMID 24124074 DOI: 10.1002/aur.1335  0.44
2014 Wong VC, Fung CK, Wong PT. Use of dysmorphology for subgroup classification on autism spectrum disorder in Chinese children. Journal of Autism and Developmental Disorders. 44: 9-18. PMID 23666520 DOI: 10.1007/s10803-013-1846-3  0.44
2013 Wong V, Cheuk DK, Lee S, Chu V. Acupuncture for acute management and rehabilitation of traumatic brain injury. The Cochrane Database of Systematic Reviews. 3: CD007700. PMID 23543554 DOI: 10.1002/14651858.CD007700.pub3  0.44
2013 Bonhoeffer J, Imoukhuede EB, Aldrovandi G, Bachtiar NS, Chan ES, Chang S, Chen RT, Fernandopulle R, Goldenthal KL, Heffelfinger JD, Hossain S, Jevaji I, Khamesipour A, Kochhar S, Makhene M, ... ... Wong V, et al. Template protocol for clinical trials investigating vaccines--focus on safety elements. Vaccine. 31: 5602-20. PMID 23499603 DOI: 10.1016/j.vaccine.2013.02.041  0.44
2013 Cheuk DK, Wong V, Wraige E, Baxter P, Cole A. Surgery for scoliosis in Duchenne muscular dystrophy. The Cochrane Database of Systematic Reviews. 2: CD005375. PMID 23450561 DOI: 10.1002/14651858.CD005375.pub3  0.44
2013 Chan V, Wong VCN. Spinal muscular atrophy in the chinese European Neurological Journal. 4.  0.44
2012 Wong V, Cheuk DK, Lee S, Chu V. Acupuncture for acute management and rehabilitation of traumatic brain injury. The Cochrane Database of Systematic Reviews. 12: CD007700. PMID 23418645  0.44
2012 Cheuk DK, Yeung WF, Chung KF, Wong V. Acupuncture for insomnia. The Cochrane Database of Systematic Reviews. 9: CD005472. PMID 22972087 DOI: 10.1002/14651858.CD005472.pub3  0.44
2012 Tsang JP, Poon WL, Luk HM, Fung CW, Ching CK, Mak CM, Lam CW, Siu TS, Tam S, Wong VC. Arginase deficiency with new phenotype and a novel mutation: contemporary summary. Pediatric Neurology. 47: 263-9. PMID 22964440 DOI: 10.1016/j.pediatrneurol.2012.06.012  0.44
2012 Kwong AK, Fung CW, Chan SY, Wong VC. Identification of SCN1A and PCDH19 mutations in Chinese children with Dravet syndrome. Plos One. 7: e41802. PMID 22848613 DOI: 10.1371/journal.pone.0041802  0.44
2012 Chan SH, Wong VC, Engel AG. Neuromuscular junction acetylcholinesterase deficiency responsive to albuterol. Pediatric Neurology. 47: 137-40. PMID 22759693 DOI: 10.1016/j.pediatrneurol.2012.04.022  0.44
2012 Martins S, Soong BW, Wong VCN, Giunti P, Stevanin G, Ranum LPW, Sasaki H, Riess O, Tsuji S, Coutinho P, Amorim A, Sequeiros J, Nicholson GA. Mutational origin of Machado-Joseph disease in the Australian Aboriginal communities of Groote Eylandt and Yirrkala Archives of Neurology. 69: 746-751. PMID 22351852  0.44
2012 Guo Y, Baum LW, Sham PC, Wong V, Ng PW, Lui CH, Sin NC, Tsoi TH, Tang CS, Kwan JS, Yip BH, Xiao SM, Thomas GN, Lau YL, Yang W, et al. Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese. Human Molecular Genetics. 21: 1184-9. PMID 22116939 DOI: 10.1093/hmg/ddr550  0.44
2012 Fung CW, Wong VCN. Paroxysmal non-epileptic movements in childhood Hong Kong Journal of Paediatrics. 17: 85-96.  0.44
2011 Cheuk DK, Wong V, Chen WX. Acupuncture for autism spectrum disorders (ASD) Cochrane Database of Systematic Reviews (Online). 9: CD007849. PMID 21901712  0.44
2011 Wong VCN. Global developmental delay - a delay in development of terminology Developmental Medicine and Child Neurology. 53: 585. PMID 21569014 DOI: 10.1111/j.1469-8749.2011.03986.x  0.44
2011 Kwan P, Wong V, Ng PW, Lui CH, Sin NC, Wong KS, Baum L. Gene-wide tagging study of the association between ABCC2, ABCC5 and ABCG2 genetic polymorphisms and multidrug resistance in epilepsy. Pharmacogenomics. 12: 319-25. PMID 21449672 DOI: 10.2217/pgs.10.183  0.44
2011 Gidudu J, Sack DA, Pina M, Hudson MJ, Kohl KS, Bishop P, Chatterjee A, Chiappini E, Compingbutra A, da Costa C, Fernandopulle R, Fischer TK, Haber P, Masana W, de Menezes MR, ... ... Wong VCN, et al. Diarrhea: Case definition and guidelines for collection, analysis, and presentation of immunization safety data Vaccine. 29: 1053-1071. PMID 21130754 DOI: 10.1016/j.vaccine.2010.11.065  0.44
2011 Wong VCN, Chung B. Value of clinical assessment in the diagnostic evaluation of Global Developmental Delay (GDD) using a Likelihood Ratio Model Brain and Development. 33: 548-557. PMID 20965674 DOI: 10.1016/j.braindev.2010.09.009  0.44
2011 Yeung WL, Wong VC, Chan KY, Hui J, Fung CW, Yau E, Ko CH, Lam CW, Mak CM, Siu S, Low L. Expanding phenotype and clinical analysis of tyrosine hydroxylase deficiency. Journal of Child Neurology. 26: 179-87. PMID 20823027 DOI: 10.1177/0883073810377014  0.44
2011 Wong VC. Authors' reply Focus On Alternative and Complementary Therapies. 16: 47-48. DOI: 10.1111/j.2042-7166.2010.01070-6.x  0.44
2011 Chan AS, Han YMY, Leung WWM, Leung C, Wong VCN, Cheung MC. Abnormalities in the anterior cingulate cortex associated with attentional and inhibitory control deficits: A neurophysiological study on children with autism spectrum disorders Research in Autism Spectrum Disorders. 5: 254-266. DOI: 10.1016/j.rasd.2010.04.007  0.44
2010 Chan SH, Wong VC, Fung CW, Dale RC, Vincent A. Anti-NMDA receptor encephalitis with atypical brain changes on MRI. Pediatric Neurology. 43: 274-8. PMID 20837307 DOI: 10.1016/j.pediatrneurol.2010.05.004  0.44
2010 Liu Y, Zou LP, Du JB, Wong V. Electro-acupuncture protects against hypoxic-ischemic brain-damaged immature rat via hydrogen sulfide as a possible mediator Neuroscience Letters. 485: 74-78. PMID 20813156 DOI: 10.1016/j.neulet.2010.08.068  0.44
2010 Wong VCN, Chen WX, Liu WL. Randomized controlled trial of electro-acupuncture for autism spectrum disorder Alternative Medicine Review. 15: 136-146. PMID 20806998  0.44
2010 Wong VCN, Sun JG. Randomized controlled trial of acupuncture versus sham acupuncture in autism spectrum disorder Journal of Alternative and Complementary Medicine. 16: 545-553. PMID 20804366 DOI: 10.1089/acm.2007.0768  0.44
2010 Woo J, Goggins W, Zhang X, Wong V, Griffiths S. Ageing and utilisation of hospital services in Hong Kong: A retrospective cohort study Hong Kong Medical Journal. 16: 4-7. PMID 20601725  0.44
2010 Wu Y, Jin Z, Li K, Lu ZL, Wong V, Han TL, Zheng H, Caspi O, Liu G, Zeng YW, Zou LP. Functional magnetic resonance imaging activation of the brain in children: real acupoint versus sham acupoint. Journal of Child Neurology. 25: 849-55. PMID 20595697 DOI: 10.1177/0883073809351314  0.44
2010 Zhang C, Wong V, Ng PW, Lui CH, Sin NC, Wong KS, Baum L, Kwan P. Failure to detect association between polymorphisms of the sodium channel gene SCN1A and febrile seizures in Chinese patients with epilepsy. Epilepsia. 51: 1878-81. PMID 20477842 DOI: 10.1111/j.1528-1167.2010.02587.x  0.44
2010 Mak CM, Lam CW, Siu TS, Chan KY, Siu WK, Yeung WL, Hui J, Wong VC, Low LC, Ko CH, Fung CW, Chen SP, Yuen YP, Lee HC, Yau E, et al. Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese. Molecular Genetics and Metabolism. 99: 431-3. PMID 20056467 DOI: 10.1016/j.ymgme.2009.12.011  0.44
2010 Wong VCN, Kwan QK. Randomized controlled trial for early intervention for Autism: A pilot study of the Autism 1-2-3 project Journal of Autism and Developmental Disorders. 40: 677-688. PMID 20020319 DOI: 10.1007/s10803-009-0916-z  0.44
2010 Ma YM, Liu TK, Wong V. Guillain-Barre syndrome in southern Chinese children: 32 year experience in Hong Kong. Pediatrics International : Official Journal of the Japan Pediatric Society. 52: 13-9. PMID 19702649 DOI: 10.1111/j.1442-200X.2009.02951.x  0.44
2009 Kwan P, Wong V, Ng PW, Lui CH, Sin NC, Poon WS, Ng HK, Wong KS, Baum L. Gene-wide tagging study of association between ABCB1 polymorphisms and multidrug resistance in epilepsy in Han Chinese. Pharmacogenomics. 10: 723-32. PMID 19450124 DOI: 10.2217/pgs.09.32  0.44
2009 Wong VCN. Use of complementary and alternative medicine (CAM) in autism spectrum disorder (ASD): Comparison of chinese and western culture (Part A) Journal of Autism and Developmental Disorders. 39: 454-463. PMID 18784992 DOI: 10.1007/s10803-008-0644-9  0.44
2009 Wong V, Cheuk DKL, Chu V. Acupuncture for hypoxic ischemic encephalopathy in neonates Cochrane Database of Systematic Reviews. DOI: 10.1002/14651858.CD007968  0.44
2009 Cheuk DKL, Wong V, Chen WX. Acupuncture for autistic spectrum disorder Cochrane Database of Systematic Reviews. DOI: 10.1002/14651858.CD007849  0.44
2009 Cheuk DKL, Wong V. Acupuncture for epilepsy Cochrane Database of Systematic Reviews. DOI: 10.1002/14651858.CD005062.pub3  0.44
2008 Chen WX, Wu-Li L, Wong VCN. Electroacupuncture for children with autism spectrum disorder: Pilot study of 2 cases Journal of Alternative and Complementary Medicine. 14: 1057-1065. PMID 18990052 DOI: 10.1089/acm.2007.0823  0.44
2008 Wu Y, Zou LP, Han TL, Zheng H, Caspi O, Wong V, Su Y, Shen KL. Randomized controlled trial of traditional Chinese medicine (acupuncture and tuina) in cerebral palsy: part 1--any increase in seizure in integrated acupuncture and rehabilitation group versus rehabilitation group? Journal of Alternative and Complementary Medicine (New York, N.Y.). 14: 1005-9. PMID 18990048 DOI: 10.1089/acm.2007.0756  0.44
2008 Wu Y, Jin Z, Li K, Lu ZL, Wong V, Han TL, Zheng H, Caspi O, Liu G, Zeng YW, Zou LP. Effect of acupuncture on the brain in children with spastic cerebral palsy using functional neuroimaging (FMRI). Journal of Child Neurology. 23: 1267-74. PMID 18984835 DOI: 10.1177/0883073808318049  0.44
2008 Kennerknecht I, Ho NY, Wong VC. Prevalence of hereditary prosopagnosia (HPA) in Hong Kong Chinese population. American Journal of Medical Genetics. Part A. 146: 2863-70. PMID 18925678 DOI: 10.1002/ajmg.a.32552  0.44
2008 Kwan P, Poon WS, Ng HK, Kang DE, Wong V, Ng PW, Lui CH, Sin NC, Wong KS, Baum L. Multidrug resistance in epilepsy and polymorphisms in the voltage-gated sodium channel genes SCN1A, SCN2A, and SCN3A: correlation among phenotype, genotype, and mRNA expression. Pharmacogenetics and Genomics. 18: 989-98. PMID 18784617 DOI: 10.1097/FPC.0b013e3283117d67  0.44
2008 Wong CL, Wong VC. Effect of acupuncture in a patient with 7-year-history of Bell's palsy. Journal of Alternative and Complementary Medicine (New York, N.Y.). 14: 847-53. PMID 18721078 DOI: 10.1089/acm.2007.0780  0.44
2008 Leung DY, Chan SS, Lau CP, Wong V, Lam TH. An evaluation of the psychometric properties of the Smoking Self-Efficacy Questionnaire (SEQ-12) among Chinese cardiac patients who smoke. Nicotine & Tobacco Research : Official Journal of the Society For Research On Nicotine and Tobacco. 10: 1311-8. PMID 18686178 DOI: 10.1080/14622200802238928  0.44
2008 Wong SS, Luk DC, Wong VC, Scheper GC, van der Knaap MS. Vanishing white matter disease: the first reported chinese patient. Journal of Child Neurology. 23: 710-4. PMID 18539998 DOI: 10.1177/0883073808314154  0.44
2008 Fong GC, Kwan P, Hui AC, Lui CH, Fong JK, Wong V. An epidemiological study of epilepsy in Hong Kong SAR, China. Seizure. 17: 457-64. PMID 18261935 DOI: 10.1016/j.seizure.2007.12.005  0.44
2008 Wong VCN, Hui SLH. Epidemiological study of autism spectrum disorder in China Journal of Child Neurology. 23: 67-72. PMID 18160559 DOI: 10.1177/0883073807308702  0.44
2008 Yam WK, Ronen GM, Cherk SW, Rosenbaum P, Chan KY, Streiner DL, Cheng SW, Fung CW, Ho JC, Kwong KL, Ma LC, Ma DK, Tsui KW, Wong V, Wong TY. Health-related quality of life of children with epilepsy in Hong Kong: how does it compare with that of youth with epilepsy in Canada? Epilepsy & Behavior : E&B. 12: 419-26. PMID 18158271 DOI: 10.1016/j.yebeh.2007.11.007  0.44
2008 Wong VCN, Hui SLH. Brief report: Emerging services for children with autism spectrum disorders in Hong Kong (1960-2004) Journal of Autism and Developmental Disorders. 38: 383-389. PMID 17605098 DOI: 10.1007/s10803-007-0394-0  0.44
2008 Wong V. Correspondence Journal of Child Neurology. 23: 719. DOI: 10.1177/0883073808314366  0.44
2008 Ip P, Wong V, Ho M, Lee J, Wong W. Environmental mercury exposure in children: South China's experience (Pediatrics International (2004) 46 (715-721) DOI: 10.1111/j.1442-200x.2004. 01972.x) Pediatrics International. 50: 606. DOI: 10.1111/j.1442-200X.2008.02709.x  0.44
2007 Wong VCN, Li SYH. Rett syndrome: Prevalence among Chinese and a comparison of MECP2 mutations of classic Rett syndrome with other neurodevelopmental disorders Journal of Child Neurology. 22: 1397-1400. PMID 18174559 DOI: 10.1177/0883073807307091  0.44
2007 Rath B, Linder T, Cornblath D, Hudson M, Fernandopulle R, Hartmann K, Heininger U, Izurieta H, Killion L, Kokotis P, Oleske J, Vajdy M, Wong V. "All that palsies is not Bell's [1]"-The need to define Bell's palsy as an adverse event following immunization Vaccine. 26: 1-14. PMID 18037542 DOI: 10.1016/j.vaccine.2007.10.043  0.44
2007 Chung BHY, Tsang AMC, Wong VCN. Neurologic complications in children hospitalized with influenza: comparison between USA and Hong Kong The Journal of Pediatrics. 151: e17-18; author reply. PMID 17961673  0.44
2007 Martins S, Calafell F, Gaspar C, Wong VC, Silveira I, Nicholson GA, Brunt ER, Tranebjaerg L, Stevanin G, Hsieh M, Soong BW, Loureiro L, Dürr A, Tsuji S, Watanabe M, et al. Asian origin for the worldwide-spread mutational event in Machado-Joseph disease. Archives of Neurology. 64: 1502-8. PMID 17923634 DOI: 10.1001/archneur.64.10.1502  0.44
2007 Fertleman CR, Ferrie CD, Aicardi J, Bednarek NA, Eeg-Olofsson O, Elmslie FV, Griesemer DA, Goutières F, Kirkpatrick M, Malmros IN, Pollitzer M, Rossiter M, Roulet-Perez E, Schubert R, Smith VV, ... ... Wong V, et al. Paroxysmal extreme pain disorder (previously familial rectal pain syndrome). Neurology. 69: 586-95. PMID 17679678 DOI: 10.1212/01.wnl.0000268065.16865.5f  0.44
2007 Wong V. Occipital deep white matter hyperintensities in autism spectrum disorder Pediatrics International. 49: 513-515. PMID 17587278 DOI: 10.1111/j.1442-200X.2007.02411.x  0.44
2007 Kwan P, Baum L, Wong V, Ng PW, Lui CH, Sin NC, Hui AC, Yu E, Wong LK. Association between ABCB1 C3435T polymorphism and drug-resistant epilepsy in Han Chinese. Epilepsy & Behavior : E&B. 11: 112-7. PMID 17521963 DOI: 10.1016/j.yebeh.2007.04.013  0.44
2007 Chung B, Wong V. Relationship between five common viruses and febrile seizure in children Archives of Disease in Childhood. 92: 589-593. PMID 17284480 DOI: 10.1136/adc.2006.110221  0.44
2007 Wong SSN, Wong VCN. Functional independence measure for children: A comparison of Chinese and Japanese children Neurorehabilitation and Neural Repair. 21: 91-96. PMID 17172559 DOI: 10.1177/1545968306290225  0.44
2006 Cheuk DKL, Wong V. Attention-deficit hyperactivity disorder and blood mercury level: A case-control study in Chinese children Neuropediatrics. 37: 234-240. PMID 17177150 DOI: 10.1055/s-2006-924577  0.44
2006 Chu MMY, Lee WC, Leung JLS, Wong V. Modified symbolic play test for Oriental children Pediatrics International. 48: 519-524. PMID 17168967 DOI: 10.1111/j.1442-200X.2006.02285.x  0.44
2006 Feuk L, Kalervo A, Lipsanen-Nyman M, Skaug J, Nakabayashi K, Finucane B, Hartung D, Innes M, Kerem B, Nowaczyk MJ, Rivlin J, Roberts W, Senman L, Summers A, Szatmari P, ... Wong V, et al. Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia American Journal of Human Genetics. 79: 965-972. PMID 17033973 DOI: 10.1086/508902  0.44
2006 Chen WX, Wong VCN, Wong KY. Neurodevelopmental outcome of severe neonatal hemolytic hyperbilirubinemia Journal of Child Neurology. 21: 474-479. PMID 16948930 DOI: 10.2310/7010.2006.00107  0.44
2006 Wong VCN, Sun JG, Yeung DWC. Pilot study of efficacy of tongue and body acupuncture in children with visual impairment Journal of Child Neurology. 21: 462-473. PMID 16948929  0.44
2006 Wong VCN, Sun JG, Yeung DWC. Pilot study of positron emission tomography (PET) brain glucose metabolism to assess the efficacy of tongue and body acupuncture in cerebral palsy Journal of Child Neurology. 21: 455-462. PMID 16948928 DOI: 10.2310/7010.2006.00101  0.44
2006 Cheuk DKL, Li SYH, Wong V. Exon 3 polymorphisms of dopamine D4 receptor (DRD4) gene and attention deficit hyperactivity disorder in Chinese children American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 141: 907-911. PMID 16917940 DOI: 10.1002/ajmg.b.30397  0.44
2006 Wong V. Study of the relationship between tuberous sclerosis complex and autistic disorder Journal of Child Neurology. 21: 199-204. PMID 16901420  0.44
2006 Wong V, Chen WX, Wong KY. Short- and long- term outcome of severe neonatal nonhemolytic hyperbilirubinemia Journal of Child Neurology. 21: 309-315. PMID 16900927 DOI: 10.1177/08830738060210040301  0.44
2006 Wong VCN, Chung BHY, Li S, Goh W, LEE SL. Mutation of Gene in Spinal Muscular Atrophy Respiratory Distress Type I Pediatric Neurology. 34: 474-477. PMID 16765827 DOI: 10.1016/j.pediatrneurol.2005.10.022  0.44
2006 Martins S, Calafell F, Wong VCN, Sequeiros J, Amorim A. A multistep mutation mechanism drives the evolution of the CAG repeat at MJD/SCA3 locus European Journal of Human Genetics. 14: 932-940. PMID 16724006 DOI: 10.1038/sj.ejhg.5201643  0.44
2006 Cheuk DKL, Wong V. Meta-analysis of association between a catechol-O-methyltransferase gene polymorphism and attention deficit hyperactivity disorder Behavior Genetics. 36: 651-659. PMID 16676224 DOI: 10.1007/s10519-006-9076-5  0.44
2006 Chan TYP, Wong V. Recurrent headache in Chinese children: Any agreement between clinician diagnosis and sympton-based diagnoses using the International Classification of Headache Disorders (second edition)? Journal of Child Neurology. 21: 132-138. PMID 16566877 DOI: 10.1177/08830738060210020101  0.44
2006 Wong V, Khong PL. Tuberous sclerosis complex: Correlation of magnetic resonance imaging (MRI) findings with comorbidities Journal of Child Neurology. 21: 99-105. PMID 16566871 DOI: 10.1177/08830738060210020901  0.44
2006 Chen WX, Wong V. Visual evoked potentials in neonatal hyperbilirubinemia Journal of Child Neurology. 21: 58-62. PMID 16551455 DOI: 10.1177/08830738060210011701  0.44
2006 Chung B, Wat LCY, Wong V. Febrile seizures in southern chinese children: Incidence and recurrence Pediatric Neurology. 34: 121-126. PMID 16458824 DOI: 10.1016/j.pediatrneurol.2005.08.007  0.44
2006 Cheuk DKL, Li SYH, Wong V. No association between VNTR polymorphisms of dopamine transporter gene and attention deficit hyperactivity disorder in Chinese children American Journal of Medical Genetics - Neuropsychiatric Genetics. 141: 123-125. PMID 16402340 DOI: 10.1002/ajmg.b.30280  0.44
2006 Wong VCN, Chung BHY. Evaluating a child with Partial Developmental Delay (ParDD), Global Developmental Delay (GDD)/mental retardation (MR): Clinical expertise based or evidence-based? Current Pediatric Reviews. 2: 143-153. DOI: 10.2174/157339606776894621  0.44
2006 Wong V. Reply from the author [8] Neurology. 66: 1456.  0.44
2005 Wong VCN, Lam CW, Fung CW. Stiff child syndrome with mutation of DYT1 gene Neurology. 65: 1465-1466. PMID 16275837 DOI: 10.1212/01.wnl.0000183153.82651.72  0.44
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